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Oncogenic Role of THOR, a Conserved Cancer/Testis Long Non-coding RNA
Author(s) -
Yasuyuki Hosono,
Yashar S. Niknafs,
John R. Prensner,
Matthew K. Iyer,
Saravana M. Dhanasekaran,
Rohit Mehra,
Sethuramasundaram Pitchiaya,
Jean C. Tien,
June EscaraWilke,
Anton Poliakov,
Shih-Chun Chu,
Sahal Saleh,
Keerthana Sankar,
Fengyun Su,
Shuling Guo,
Yuanyuan Qiao,
Susan M. Freier,
Huynh-Hoa Bui,
Xuhong Cao,
Rohit Malik,
Timothy M. Johnson,
David G. Beer,
Felix Y. Feng,
Weibin Zhou,
Arul M. Chinnaiyan
Publication year - 2017
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2017.11.040
Subject(s) - biology , zebrafish , ectopic expression , gene knockdown , transcriptome , genetics , cancer research , computational biology , gene , gene expression
Large-scale transcriptome sequencing efforts have vastly expanded the catalog of long non-coding RNAs (lncRNAs) with varying evolutionary conservation, lineage expression, and cancer specificity. Here, we functionally characterize a novel ultraconserved lncRNA, THOR (ENSG226856), which exhibits expression exclusively in testis and a broad range of human cancers. THOR knockdown and overexpression in multiple cell lines and animal models alters cell or tumor growth supporting an oncogenic role. We discovered a conserved interaction of THOR with IGF2BP1 and show that THOR contributes to the mRNA stabilization activities of IGF2BP1. Notably, transgenic THOR knockout produced fertilization defects in zebrafish and also conferred a resistance to melanoma onset. Likewise, ectopic expression of human THOR in zebrafish accelerated the onset of melanoma. THOR represents a novel class of functionally important cancer/testis lncRNAs whose structure and function have undergone positive evolutionary selection.

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